This is an interactive session to introduce the concepts of modelling vector-borne diseases. The motivation for modelling and differences compared to modelling diseases spread by direct transmission will be covered. We will write down a basic model and derive the expression for \(R_0\).
This session is divided into three parts:
Part 1 covers:
Part 2 covers:
Part 3 covers:
We recommend saving your text at the end of each part by printing the file.
Unlike diseases that spread directly from person to person, vector-borne diseases are those diseases in which the spread of an infectious pathogen occurs via a vector — a living organism such as a mosquito. Examples of vectors include (left to right) mosquitoes, ticks, blackflies and fleas:
There are many different types of vector. While some diseases, such as malaria, are exclusively spread by a single vector genus, others, such as lymphatic filariasis, can be transmitted by multiple species. Similarly, some vectors are able to spread multiple diseases.
| Vector | Disease |
|---|---|
| Mosquito – Anopheles | Malaria, Lymphatic filariasis |
| Mosquito – Aedes | Zika, Dengue, Lymphatic filariasis |
| Mosquito – Culex | West Nile fever, Japanese encephalitis, Lymphatic filariasis |
| Blackflies | Onchocerciasis |
1.1 Do you know which of these vector-borne diseases is important to your country? Are there any others?
We can divide vector-borne diseases into two categories, those that spread by a human-vector-human cycle (e.g. malaria, dengue, zika, onchocerciasis) and those that involve a non-human host (e.g. West Nile virus, Japanese encephalitis). In this session, we will only be working with diseases that spread by a human-vector-human cycle.
Diseases spread by vectors account for almost one-fifth of all infectious diseases and are responsible for more than 700,000 deaths annually. Much of this disease burden is due to malaria and dengue infections, estimated to cause more than 440,000 deaths per year. The map below displays the distribution of deaths due to vector-borne diseases, estimated by the World Health Organization in 2002. While Africa has the highest burden, there is substantial burden in the Asia Pacific region. As global temperatures increase, the global distribution of vectors is changing, which may allow the spread of vector-borne diseases into new areas.
In this part of the session, we will consider the mechanistic process by which vector-borne diseases spread and consider the other elements that are needed in vector-borne disease models.
While there are many different types of vectors, in this and the following part we will cover modelling of diseases that are spread by mosquitoes. Female mosquitoes bite humans to obtain protein from blood for their developing eggs. These bites can transmit infection from mosquito to human or from human to mosquito. The following diagram outlines a simple transmission cycle of a mosquito-borne disease:
The steps involved in transmission, as indicated on the diagram above are:
You might notice that in our diagram above both humans and mosquitoes are infectious immediately upon being infected. In reality, it takes time for the infectious load to build in a host before they are capable of transmitting infection. We make this assumption here to simplify the explanation of the transmission process.
For the model that we are building in this session, we will assume that:
The feature that makes vector-borne disease models different to models for diseases spread by direct contact is that the human and mosquito populations interact through bites. We start with the assumption that each mosquito makes a fixed number of bites per unit time, and we define this as \(b\). We further assume that those bites are uniformly spread across the human population, \(N_H\). It follows that the rate at which a specific human is bitten by a specific mosquito, which we define as \(r\), can be calculated as:
\[r=\frac{b}{N_H}\]
This is the number of bites a single human receives from a single mosquito per unit time, and is analogous to ‘contact’ in directly-transmitted disease models.
2.3 What happens to the rate \(r\) as the human population increases? What do you think might be the implication for transmission?
Similar to contacts in the case of directly transmitted (human to human) infections, not all mosquito bites will be of sufficient intensity to transmit infection. For each bite, we assign a probability that the bite is of sufficient intensity to transmit infection (if one host is susceptible and the other infectious), using the following notation:
We refer to this as the probability of successful transmission.
2.4 Write the expression for the number of bites a single human receives from a single mosquito per unit time that are capable of transmitting infection from mosquito to human.
The expressions in 2.4 and 2.5 are for the rate of ‘successful’ bites between a single susceptible human and a single infectious mosquito. The force of infection on humans, \(λ_H\), is the rate at which a susceptible human acquires infection, noting that infection can be acquired from any infectious mosquito.
2.6 Write the expression for the force of infection on humans, \(λ_H\).
Similarly the force of infection on mosquitoes, \(λ_M\), is the rate at which a susceptible mosquito acquires infection. A mosquito can acquire infection from any infectious human.
2.7 Write the expression for the force of infection on mosquitoes, \(λ_M\).
The force of infection (on humans or mosquitoes) is the rate at which infection is acquired in a single susceptible host. To calculate the rate that new infections occur in the whole human or mosquito population, we have to multiply the force of infection by the population at risk of being infected.
2.8 Using the equation for the force of infection on humans, \(λ_H\), write the expression for the total number of human infections per unit time.
Now that we have explored how the human and mosquito populations interact in a vector-borne disease model and made some assumptions around what to include in our first model, we will design an appropriate model structure. Using the model compartments you identified in Part 2, and the inflows and outflows from each compartment required based on the assumptions discussed in Part 2, draw your proposed model structure.
Instructions:
You can draw a diagram electronically in a program such as PowerPoint, or you can draw your diagram by hand and take a photo
Make sure you label all compartments as well as the inflows and outflows from each compartment.
Save your diagram in one of the following formats: .jpg, .gif, .png
Upload your diagram using the Browse… button below
If you prefer, you can describe your model in words in the space below
NB: You can replace a file by clicking on the file name and selecting a file with a different name.
The basic reproduction number, \(R_0\), for a vector-borne disease is the number of secondary infections of the same type (i.e. vector or human) generated by a single infectious vector or human in a totally susceptible population. Let’s start with a single infectious mosquito.
We firstly start with the expected number of humans (in a totally susceptible population) infected by this mosquito over the duration of their infectious period.
3.4 Write down this expression using the information you have developed in Parts 2 and 3 (i.e. number of new infections and the duration of the infectious period). We will denote this as \(R_{HM}\).
Next we consider the expected number of mosquitoes (in a totally susceptible population) infected by a single human over the duration of their infectious period.
3.5 Write down this expression using the information you have developed in Parts 2 and 3 (i.e. number of new infections and the duration of the infectious period). We will denote this as \(R_{MH}\).
Since a single mosquito infects \(R_{HM}\) humans, and each of these humans infects \(R_{MH}\) mosquitoes, the number of secondary infections a mosquito generates in mosquitoes is the product of \(R_{HM}\) and \(R_{MH}\).
3.6 Write down this expression, cancelling terms where possible to simplify the expression.